Allele Registry

Canonical Allele Identifier: PA103296

Gene: F11 HGNC NCBI

ClinVar Allele:

26943

ClinVar RCV:

RCV000012679

ClinVar Variation:

11904

HGVS (amino-acid)	Matching Registered Transcripts
NP_000119.1:p.Trp587Ser	CA121769 NM_000128.4:c.1760G>C